In a high pressure sodium vapor lamp, sufficiently small quantities of sodium and mercury are inserted therein so that all of the added sodium and mercury will be vaporized when the lamp is operated. The quantities are so selected that a completed lamp exhibits high efficiency, remarkable color rendition and durability. Also, the lamp can produce a suitable arc voltage by means of a less expensive ballast. The small quantity of sodium added is accurately controlled by decomposing sodium azide nan3. The small quantity of mercury is accurately controlled by decomposing Ti-Hg alloy or Al-Zr-Ti-Hg alloy.
|
1. A method of fabricating a sodium vapor lamp of the type having an arc tube made of a heat-resistant and light transmissive tubular body with sodium, mercury and a starting gas therein, whereby all of the filled sodium and mercury are vaporized when operated, comprising the steps of: placing an amount of sodium azide nan3 in the range of 0.020 to 0.153 mg per cubic centimeter of volume of said arc tube in communication with the interior of said arc tube, sealing off said nan3 from the atmosphere, heating said nan3 to decompose it into sodium and nitrogen, and withdrawing the resultant nitrogen from said tube.
2. A method as claimed in
3. A method as claimed in
4. A method as claimed in
|
|||||||||||||||||||||||||
This is a division of application Ser. No. 679,288, filed Apr. 21, 1976, now U.S. Pat. No. 4,075,520.
The present invention relates to a method for fabricating sodium vapor lamps of unsaturated vapor pressure type.
High pressure sodium vapor lamps, which constitute one known type of saturated vapor pressure electric discharge lamps, are known in the art. Those which are commercially available are filled with large amounts of sodium and mercury, and parts thereof become accumulated in the liquid phase as an amalgam at the coolest points within the arc tube of the lamp. In such lamps, the operating characteristics, especially the arc voltage, tend to fluctuate depending on those factors which will affect the temperature of the coolest point in the arc tube. One factor, for example, would be a variation of the source voltage.
It is theoretically known that the above shortcoming can be overcome by limiting the amount of sodium and mercury to that which will become totally vaporized. In this connection it is possible to work out by calculation, the maximum allowable amount of the sodium and mercury, i.e. the maximum amount which would not result in the condensation of the substances under working condition.
Despite the latter, no one has previously been able to discover and disclose the appropriate amount of fillers (i.e. sodium and mercury) to be used for a practical electric discharge lamp having high efficiency, acceptable color rendition, long service life and suitable stabilized arc voltage using an economical ballast. This is attributable to the fact that the appropriate amount of fillers is extremely small and that sodium is one of the chemically active elements. It is quite difficult to pick up and accurately fill such a small amount of chemically active sodium without being contaminated by other atmospheric elements such as oxygen or moisture. At the same time, it is very difficult to form a very small drop of mercury on an industrial scale, since mercury has a large surface tension and a large specific gravity.
It is therefore an object of the present invention to overcome the difficulty to fill in very small amount of sodium and mercury quantitatively without any contamination. Sodium is added by decomposing sodium azide NaN3 in the arc tube space. The amount of sodium azide is limited to the range of between 0.020 mg and 0.153 mg per cubic centimeter of the volume of the arc tube, thereby providing a practically usable high pressure sodium vapor lamp satisfying all requirements for high intensity electric discharge lamp. Mercury is added by decomposing Ti-Hg alloy or Al-Zr-Ti-Hg alloy in the arc tube space with sodium azide NaN3.
FIG. 1 is a partially sectioned side elevation view of a high pressure sodium arc tube according to the present invention during an intermediate stage of manufacture.
FIG. 2 is a partially sectioned side elevation of a completed arc tube according to the present invention.
FIG. 3 is a graph showing the relation of lamp current to lamp voltage for high pressure sodium arc tubes of the prior art and of the present invention.
Referring to FIG. 1, a light transmissive tubular ceramic body 1, which may be a polycrystalline alumina tube or a monocrystalline sapphire tube, is closed at the ends thereof by closing discs 2, 2' of a similar alumina material. The closing discs 2, 2' have respective central openings through which niobium exhaust tubes 3, 3' pass. A tungsten electrode 4 is provided at the inner ends of each of the exhaust tubes 3, 3'. The closing disc, exhaust tube and alumina tube are secured hermetically with one another by means of sealing glass.
Sodium and mercury are introduced into the arc tube 1 via exhaust tube 3 in a manner to be described hereafter.
It has been found to be quite effective to make use of the thermal decomposition of sodium azide (NaN3) to fill the arc tube with the specified amount of sodium in a pure state. Sodium azide, which is a white powder and is stable under atmospheric conditions, decomposes to free sodium and nitrogen (N2) when heated to 400°C It is possible to feed a controlled quantity of very pure sodium to the arc tube by generating the latter reaction within the arc tube after having insulated the arc tube from the outer atmosphere.
It is very difficult to produce very small particles of mercury of a specific amount. For this purpose however, the thermal decomposition of Titanium-Mercury alloy (Ti-Hg alloy) or Aluminum-Zirconium-Titanium-Mercury alloy (Al-Zr-Ti-Hg alloy), as disclosed in U.S. Pat. No. 3,203,901 and now commercially available as the Mercury Dispenser, can be effectively utilized. The latter alloy can be obtained in the form of a powder molded piece, and separates mercury therefrom at a predetermined rate when heated up to 700°C The thermal decomposition reaction of the alloy is also obtainable within the arc tube so that a specific predetermined amount of mercury may be entered into the tube.
As a suitable solvent for sodium azide (NaN3), methyl alcohol is preferably used for convenience of the succeeding drying process although sodium azide is also soluble in water. As an example 0.5 g of NaN3 was dissolved in 100 ml of methyl alcohol, and 0.04 ml of the resulting solution was used for one 400 Watt arc tube. The solution was first placed into a filler container or injector 8. The filler container 8 may be of a heat resistant material, such as stainless steel, formed in a tumbler like shape or an elongated tubular shape with one end being closed. After the solvent methyl alcohol dries up, precisely 0.2 mg (500 × 0.04/100) of NaN3 remained in the filler container 8.
Thereafter, 10 mg of Mercury Dispenser, consisting of the Al-Zr-Ti-Hg alloy, was placed into the container 8 to form a mixture 9 with NaN3. The container 8 was then inserted into the exhaust pipe 3, and the open end thereof was closed by welding and pressing. The other exhaust pipe 3' was connected to an exhaust system (not shown) to evacuate the space within the arc tube. The end portion of the exhaust pipe 3 where the container 8 is positioned was heated to 400°C, and the NaN3 decomposed to generate Na and free N2. (2NaN3→2Na + 3N2 ) Thus, 0.07 mg of Na was generated from 0.2 mg of NaN3, and the simultaneously generated free N2 was exhausted through the exhaust pipe 3'. This can be easily accomplished due to the extreme difference in boiling points of nitrogen and NaN3. It is a simple matter to maintain the temperature of the exhaust pipe such that the N2 is in a vapor state while the NaN3 is in a liquid state. Subsequent heating of the exhaust pipe 3 to 700°C caused 2 mg of mercury to separate from the Mercury Dispenser. The sodium and mercury thus obtained were vaporized to escape from the exhaust pipe 3, but were condensed within the arc tube by keeping the arc tube cool during the process. A starting gas, for example 20 Torr or Xenon, was introduced through the exhaust pipe 3'. The exhaust pipes 3, 3' were then pinched off at suitable lengths and closed.
Although it will be understood by those skilled in the art that some modifications may be made in the sequence and the manner of above described process, the filling of sodium and mercury into the art tube is accomplished by making use of sodium azide and Mercury Dispenser, with precise control in quantity and without being contaminated by atmospheric impurities.
It is strictly required for the high pressure sodium vapor lamp of unsaturated vapor pressure type, that all of the sodium and mercury be perfectly vaporized. For this purpose, the thermal conditions within the arc tube must be regulated. Specifically the ends or the arc tube, which are the coolest points therein, must be maintained at a temperature high enough to assure the complete vaporization of the filled substances. A heat insulating sleeve is provided to solve the problem.
Referring now to FIG. 2, sheets 5, 5' of a refractory and insulating packing material are placed around the end portions of the arc tube 1. Then, metal bands 6, 6' are wound around the packing material 5, 5'. The opposing circumferential ends 7, 7' of respective metal bands 6, 6' are brought together and secured to each other by means of spot welding in such a manner that the arc tube 1 is held tightly by the metal bands 6, 6' through the medium of the packing materials 5, 5'. The heat insulating sleeve is thus held onto the arc tube.
The completed arc tube is then mechanically suspended in an outer jacket or bulb by conventional means, and thereafter required electrical connection is made to provide a high pressure sodium vapor lamp of the invention which is similar in appearance with the conventional ones.
Referring now to FIG. 3, the lamp current versus lamp voltage is shown for a conventional 400 watt high pressure sodium vapor lamp and for a 400 watt lamp made as described above. The curve b is for the conventional lamp, and it can be seen that the lamp voltage increases as the lamp current increases, and the rate of the increase becomes larger as the current increases. Referring to the curve a, which represents the characteristic of a lamp according to the present invention, at the lower currents the lamp voltage increases as the current increases at a rate greater than that in the conventional lamp. However, for increases of the lamp current above the point C., the lamp voltage does not increase and is maintained substantially constant. This is attributable to the fact that the vapor pressure is maintained substantially constant after all of the filled sodium and mercury have been vaporized perfectly.
The point D defined by 110V of lamp voltage and 4.3 A of lamp current shows the rating point of the lamp having lamp output of 400 Watt.
The lamp voltage Vsa under unsaturated vapor pressure varies depending on the quantity of sodium and mercury in the arc tube. The lamp voltage Vsa increases as the quantity of sodium increases, accompanied by the change in spectral characteristic and efficiency, while an increase in quantity of mercury does not affect the spectral characteristic materially. However it also raises the lamp voltage Vsa. Therefore, it is preferable to select the quantity of sodium first to obtain a practically acceptable efficiency and color, and then to determine the quantity of mercury so as to obtain a suitable lamp voltage Vsa.
An economical lamp voltage Vsa is within the range of 70 to 140 V, and more particular in the range of 90 to 130 V.
The volume of the 400 watt arc tube according to the above example was about 5.6 cm3. Thus, the quantities of sodium and mecury in the tube were 0.0126 mg and 0.357 mg, respectively, for every cubic centimeter of the tube volume.
The quantity of sodium is, preferably, 0.007 to 0.054 mg for every cubic centimeter, because the efficiency is unacceptably low for smaller quantities and the durability of the arc tube is reduced for larger quantities of sodium. The above described range of 0.007 to 0.054 mg provides almost the same color as the conventional lamps. The range of amount of NaN3 between 0.020 to 0.152 mg corresponds to the range of sodium between 0.007 to 0.054 mg because the yield of the decomposition reaction is quantitative.
The quantity of mercury is selected, as a rule, in inverse proportion to the quantity of sodium, for the purpose of obtaining the suitable lamp voltage Vsa.
The following Table I is the result of tests, wherein lamps of 400 W, filled by different quantities of sodium and mercury are measured under 400 W output.
| Table 1 |
| ______________________________________ |
| lamp lamp |
| quantity mg/cm3 |
| voltage current efficiency |
| No. Na Hg V A lm/W color |
| ______________________________________ |
| 1 0.0126 0.357 110 4.3 110 yellow- |
| white |
| 2 0.0126 0.803 153 3.1 92 pink |
| 3 0.0315 0.178 120 4.0 105 yellow- |
| white |
| 4 0.0315 1.07 220 2.2 80 pink |
| ______________________________________ |
Takatsuka, Kenji, Furukubo, Haruo, Takeji, Yasaburo
| Patent | Priority | Assignee | Title |
| 4950953, | Nov 30 1987 | Kabushiki Kaisha Toshiba | High pressure sodium lamp with sodium amalgam of controlled amount sealed therein |
| 5022882, | Mar 10 1983 | GTE Products Corporation | Arc tube dosing process for unsaturated high pressure sodium lamp |
| 5026311, | Mar 10 1983 | GTE Products Corporation | Arc tube fabrication process |
| 5192239, | Nov 27 1990 | Patent Treuhand Gesellschaft fur elektrische Gluhlampen m.b.H. | Method and apparatus to make a discharge vessel for a sodium high-pressure discharge lamp |
| 5387837, | Mar 27 1992 | U.S. Philips Corporation | Low-pressure discharge lamp and luminaire provided with such a lamp |
| Patent | Priority | Assignee | Title |
| 2465062, | |||
| 3093430, | |||
| 3203901, | |||
| 3315116, | |||
| 3453477, | |||
| 3788724, | |||
| 3957328, | Mar 16 1973 | U.S. Philips Corporation | Method of manufacturing a mercury vapour discharge lamp |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| Sep 06 1977 | Japan Storage Battery Company Limited | (assignment on the face of the patent) | / |
| Date | Maintenance Fee Events |
| Date | Maintenance Schedule |
| May 29 1982 | 4 years fee payment window open |
| Nov 29 1982 | 6 months grace period start (w surcharge) |
| May 29 1983 | patent expiry (for year 4) |
| May 29 1985 | 2 years to revive unintentionally abandoned end. (for year 4) |
| May 29 1986 | 8 years fee payment window open |
| Nov 29 1986 | 6 months grace period start (w surcharge) |
| May 29 1987 | patent expiry (for year 8) |
| May 29 1989 | 2 years to revive unintentionally abandoned end. (for year 8) |
| May 29 1990 | 12 years fee payment window open |
| Nov 29 1990 | 6 months grace period start (w surcharge) |
| May 29 1991 | patent expiry (for year 12) |
| May 29 1993 | 2 years to revive unintentionally abandoned end. (for year 12) |